A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17374852



Internal ID22600521
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:73016333..73062039hg38UCSC Ensembl
chr17:71012472..71058178hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg3845707
hg1945707
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5931229
Supporting Variants
Samples
Known GenesSLC39A11
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17374852
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer